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dbVar

Database of genomic structural variation

nsv5672467

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Ebert et al. 2021

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 135 SVs from 36 studies. See in: genome view

Submitted genomic32,147,902-32,147,902

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5672467	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000022.11	Chr22	32,147,902	32,147,902
nsv5672467	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000022.10	Chr22	32,543,889	32,543,889

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17133062	insertion	HG03065	Sequencing	Sequence alignment	3,836

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17133062	Submitted genomic		NC_000022.11:g.321 47902_32147903ins5 1	GRCh38 (hg38)		NC_000022.11	Chr22	32,147,902	32,147,902
nssv17133062	Remapped	Perfect	NC_000022.10:g.325 43889_32543890ins5 1	GRCh37.p13	First Pass	NC_000022.10	Chr22	32,543,889	32,543,889

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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